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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 717211생성일: 2026년 10월 24일

Propargyl alcohol → (3-Phenyl-5-isoxazolyl)methanol

https://huagongshe.com/ko/reaction/717211

반응식

참여 물질

역할이름HCID투입량
반응물Propargyl alcoholHCID 7859—
반응물TriethylamineHCID 8471—
반응물(Z)-Benzaldehyde oximeHCID 12143—
반응물ChlorosuccinimideHCID 31398—
용매DichloromethaneHCID 6344—
생성물(3-Phenyl-5-isoxazolyl)methanolHCID 276341776.8%

반응 단계

10.0 mmol of benzaldehyde oxime and 30 mL of dry dichloromethane were placed in a 250 mL single-necked round-bottom flask. 1.60 g (12.0 mmol) of N-chlorosuccinimide (NCS) was added under stirring. After NCS was completely dissolved by slightly heating, 0.56 g (10.0 mmol) of 2-propyn-1-ol was added dropwise, and then 20 mL solution of 10.1 g (10.0 mmol) of triethylamine in dichloromethane. After the addition was complete, the system was refluxed. After the completion of the reaction monitored by TLC, the mother liquor was washed with water, dried over anhydrous sodium sulfate, and separated by column chromatography (Vpetroleum ether:Vethyl acetate=5:1-2:1) to give 3-phenyl-5-hydroxymethyl-isoxazole in 76.8% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09193718B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-5429e1783feb4fff95493802e03cf19a
출처 메모uspto-grants-2015_11